Neurologic disorders in a case of Werner's syndrome;Complications neurologiques dans un cas de syndrome de Werner

Revue Neurologique

Volumn 152, Issue 10, 1996, Pages 634-636

  Just, A ^a   Canaple, S ^a   Joly, H ^a   Piussan, C ^a   Rosa, A ^a  

^a AMIENS UNIVERSITY HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

IMMUNOGLOBULIN G;

ADULT; ARTICLE; CASE REPORT; CENTRAL NERVOUS SYSTEM; CEREBROSPINAL FLUID; HEMIPLEGIA; HUMAN; MALE; MUSCLE ATROPHY; NEUROPATHY; NUCLEAR MAGNETIC RESONANCE; PERIPHERAL NERVOUS SYSTEM; WERNER SYNDROME;

ADULT; AGING; HUMANS; MALE; NERVOUS SYSTEM DISEASES; WERNER SYNDROME;

EID: 0029841045     PISSN: 00353787     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (11)

1. EPSTEIN C., MARTIN G., SCHULTZ A. (1966). Werner's syndrome. Medicine, 45 : 177-221.
2. GOTO M., HORIUCHI Y. (1978). Werner's syndrome : analysis of 15 cases with a review of the japanese literature. J Am Geriatr Soc, 26 : 341-347.
3. GOTO M., RUBEINSTEIN M., WEBER J. (1992). Genetic linkage of Werner's syndrome to five markers on chromosome 8. Nature, 355 : 735-738.
4. HAUSTEIN J., PAWLAS U., CERVOS-NAVARRO J. (1989). The Werner syndrome : a case study, Clin Neuropathol, 8: 147-151.
5. ISHII T., HOSODA Y., HAMADA Y. (1985). Pathology of the Werner syndrome. Adv Exp Med Biol, 190: 187-218.
6. KAKIGI R., ENDO C., NESHIGE R. (1992). Accelerated aging of the brain in Werner's syndrome. Neurology, 42 : 922-924.
7. MURATA K., NAKASHIMA H. (1982). Werner's syndrome : twenty four cases with a review of the japanese medical literature. J Am Geriatr Soc, 30 : 303-308.
8. SUMI S.M. (1985). Neuropathology of the Werner syndrome. Adv Exp Med Biol, 190 : 215-218.
9. UMEHARA F., ABE M., NAKAGAWA M. (1993). Werner's syndrome associated with spastic paraparesis and peripheral neuropathy. Neurology, 43 : 1252-1254.
10. WERNER O. (1904). Uber Katarakt in verbindung mit sklerodermie. Kiel, Schmidt & Klarnig, edit.
11. YU C.E., OSHIMA J., GODDARD K. (1994). Linkage disequilibrium and haplotype studies of chromosome 8p11.1-21.1 markers and Werner syndrome. Am J Hum Genet, 55 : 356-364.